EP2727582B1 - Pharmaceutical aerosol formulations of formoterol and beclometasone dipropionate - Google Patents

Pharmaceutical aerosol formulations of formoterol and beclometasone dipropionate Download PDF

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Publication number
EP2727582B1
EP2727582B1 EP14153337.2A EP14153337A EP2727582B1 EP 2727582 B1 EP2727582 B1 EP 2727582B1 EP 14153337 A EP14153337 A EP 14153337A EP 2727582 B1 EP2727582 B1 EP 2727582B1
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EP
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Prior art keywords
formulation
beclometasone dipropionate
comprised
formulation according
fumarate dihydrate
Prior art date
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EP14153337.2A
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German (de)
English (en)
French (fr)
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EP2727582A1 (en
Inventor
Gaetano Brambilla
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Chiesi Farmaceutici SpA
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Chiesi Farmaceutici SpA
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Application filed by Chiesi Farmaceutici SpA filed Critical Chiesi Farmaceutici SpA
Priority to SI201031156A priority Critical patent/SI2727582T1/sl
Priority to EP14153337.2A priority patent/EP2727582B1/en
Priority to MEP-2016-85A priority patent/ME02398B/me
Priority to PL14153337T priority patent/PL2727582T3/pl
Publication of EP2727582A1 publication Critical patent/EP2727582A1/en
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Publication of EP2727582B1 publication Critical patent/EP2727582B1/en
Priority to HRP20160630TT priority patent/HRP20160630T1/hr
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/10—Dispersions; Emulsions
    • A61K9/12—Aerosols; Foams
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/007—Pulmonary tract; Aromatherapy
    • A61K9/0073—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy
    • A61K9/008—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy comprising drug dissolved or suspended in liquid propellant for inhalation via a pressurized metered dose inhaler [MDI]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/16—Amides, e.g. hydroxamic acids
    • A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • A61K31/167—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/537—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines spiro-condensed or forming part of bridged ring systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
    • A61K31/57—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
    • A61K31/573—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone substituted in position 21, e.g. cortisone, dexamethasone, prednisone or aldosterone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00

Definitions

  • the present invention relates to pharmaceutical formulations for use in the administration of medicaments by inhalation.
  • this invention relates to a pharmaceutical formulation comprising beclometasone dipropionate and a formoterol salt for use in pressurized metered dose inhalers (MDI's).
  • MDI's pressurized metered dose inhalers
  • the invention also relates to the methods for the preparation of said pharmaceutical formulations and to the use thereof in therapy.
  • Pressurized metered dose inhalers are well known devices for administering pharmaceutical active ingredients to the respiratory tract by inhalation. They consist of containers containing multiple doses, e.g. tens or even hundreds of doses, and each of these doses is delivered by a suitable metering valve.
  • Formulations for pMDI's typically consist of suspensions or solutions of one or more active substances in a liquefied propellant which is utilized to expel respectively solid particles or droplets containing the active ingredient to the respiratory tract as an aerosol.
  • HFAs hydrofluoroalkanes
  • HFCs hydrofluorocarbons
  • HFA 134a 1, 1, 1,2-tetrafluoroethane
  • HFA 227) 1, 1, 1, 2, 3, 3, 3-heptafluoropropane
  • MMAD mass median aerodynamic diameter
  • Respirable particles are generally considered to be those with a MMAD less than 5 micron.
  • Active substances commonly delivered by inhalation include bronchodilators such as beta-2 adrenoreceptor agonists and anticholinergics, corticosteroids, anti-allergics and other active ingredients that may be efficiently administered by inhalation, thus increasing the therapeutic index and reducing side effects of the active material.
  • Formoterol i. e. 2'-hydroxy-5'-[(RS)-1-hydroxy-2 ⁇ [(RS)-p-methoxy- ⁇ - methylphenethyl] amino ⁇ ethyl] formanilide, particularly its fumarate salt, is a well known beta-2 adrenoreceptor agonist currently used clinically in the treatment of bronchial asthma and related disorders.
  • Beclometasone dipropionate is a potent anti-inflammatory steroid, named (8 S, 9 R, 10 S, 11 S ,13 S ,14 S ,16 S ,17 R )-9-chloro-11-hydroxy-10,13,16-trimethyl-3-oxo-17-[2-(propionyloxy)acetyl]-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3 H- cyclopenta[ ⁇ ]phenanthren-17-yl propionate, available under a wide number of brands for the prophylaxis and/or treatment of inflammatory respiratory disorders.
  • pMDI's pressurised metered dose inhalers
  • the currently marketed formulation contains both active ingredients dissolved in a mixture of HFA134a and ethanol as co-solvent.
  • the volumetric contribution of suspended drug particles is absent and much finer liquid droplets clouds, largely defined by the drug concentration in the solution, are generated.
  • the major advantage of said solution formulation is related to the presence of the corticosteroid in solution as the fine droplets exhibit an improved lung deposition and improved penetration into the bronchioloalveolar distal part of the respiratory tree wherein inflammation is known to play a role in spontaneous exacerbations of asthma symptoms.
  • the amount of ethanol useful for solubilising the corticosteroid may not be appropriate or optimal for ensuring the physical stability of a suspended drug. It is indeed well known that if the suspended drug has a slight solubility in the medium, a process known as Ostwald ripening can lead to particle size growth. The effect of Ostwald ripening may be particularly severe for a drug such as formoterol which need to be formulated in low doses.
  • the invention provides a pharmaceutical aerosol formulation for use in pMDIs comprising:
  • the invention provides a pressurized metered dose inhaler (pMDI) comprising a canister filled with the pharmaceutical formulation of the invention, and a metering valve for delivering a therapeutically effective dose of the active ingredients.
  • pMDI pressurized metered dose inhaler
  • the invention comprises a method of preventing and/or treating an inflammatory or obstructive airways disease such as asthma or chronic obstructive pulmonary disease (COPD) in a mammal, which comprises administration by inhalation of an effective amount of the formulation described before.
  • an inflammatory or obstructive airways disease such as asthma or chronic obstructive pulmonary disease (COPD)
  • COPD chronic obstructive pulmonary disease
  • the invention is directed to the use of a corticosteroid for aerosol formulation for inhalation comprising a formoterol pharmaceutically acceptable salt or solvate as an active ingredient and a mixture of HFA134 and ethanol as vehicle, for decreasing the solubility of said formoterol salt in said vehicle wherein the vehicle has a polarity expressed as dielectric constant ⁇ m comprised between about 9.5 and about 11.0, preferably between about 9.5 and about 10.5.
  • the corticosteroid is advantageously selected from the group of beclometasone dipropionate and solvates thereof, budesonide and epimers thereof, fluticasone and esters thereof such as propionate and furoate, mometasone furoate, flunisolide and ciclesonide, preferably beclometasone dipropionate.
  • active drug active drug
  • active ingredient active ingredient
  • active compound active compound
  • active substance active substance
  • therapeutic agent therapeutic agent
  • Formoterol includes two asymmetric centers and hence may exist in form of four different stereoisomers; furthermore its fumarate salt may exist in two different stoichiometries, e.g. 1:1 and 2:1.
  • formoterol fumarate refers to the salt in which formoterol can be each of the possible isomer either in substantially pure form or admixed in any proportions, preferably as a racemic mixture of the (R,R) and (S,S) stereoisomers.
  • % w/w and % w/v mean the weight percentage of the component with respect to the total weight or the total volume of the composition, respectively.
  • the “% w/w” corresponding to the "% w/v” can be calculated by determining the density of the vehicle.
  • “Daily therapeutically effective dose” means the quantity of active ingredient administered at one time by inhalation upon actuation of the inhaler.
  • Actuation means the release of the active ingredient from the device by a single activation (e.g. mechanical or breath).
  • Mass median aerodynamic diameter means the diameter of 50 percent by weight of the aerosolized particles upon actuation of the inhaler.
  • Co-solvent means a substance having a higher polarity than that of the propellant.
  • “Chemically stable formulation” means a formulation wherein the stability and the shelf-life of the active ingredient meet the requirements of the ICH Guideline Q1A referring to "Stability Testing of new Active Substances (and Medicinal Products)”.
  • “Physically stable” refers to formulations in which the suspended active ingredient exhibits substantially no growth in particle size over a prolonged period, are readily redispersible and, upon redispersion, do not flocculate so quickly as to prevent its constant dosing.
  • Respirable fraction refers to an index of the percentage of active particles which would reach the deep lungs in a patient.
  • the respirable fraction also termed fine particle fraction, is evaluated using a suitable in vitro apparatus such as Multistage Cascade Impactor or Multi Stage Liquid Impinger (MLSI) according to procedures reported in common Pharmacopoeias. It is calculated by the ratio between the respirable dose and the delivered dose.
  • MLSI Multi Stage Liquid Impinger
  • the delivered dose is calculated from the cumulative deposition in the apparatus, while the respirable dose (fine particle dose) is calculated from the deposition on Stages 3 (S3) to filter (AF) corresponding to particles ⁇ 4.7 microns.
  • mild persistent asthma is defined as a form characterized by less than twice a week daily symptoms, less than twice a months nocturnal asthma symptoms, and a forced expiratory volume in one second (FEV 1 ) higher than 80% with a variability comprised between 20 and 30%.
  • ⁇ m % solvent 1 / 100 ⁇ 1 + % solvent 2 / 100 ⁇ 2 + ... % solvent n / 100 ⁇ n
  • the dielectric constants of pure HFA 134a and ethanol are respectively 9.51 and 25.7 (Solvay Solkane ® HFA13a monograph; Duncan Q et al Dielectric Analysis of Pharmaceutical Systems, 1995, Taylor and Francis, Lond on).
  • concentrations expressed as w/w are approximate in that they do not compensate for the density mismatch between HFA13a and ethanol. However, the precise values may be readily determined by the skilled person.
  • the present invention provides a pharmaceutical aerosol formulation for use in pMDIs comprising:
  • the formulation comprises as active ingredients only the combination of formoterol salt and beclometasone dipropionate.
  • the formoterol salt is preferably present as a racemic mixture of the (R,R) and (S,S) stereoisomers. It is also preferably present in a crystalline form, more preferably with a crystallinity degree higher than 95%, even more preferably higher than 98%, as determined according to known methods.
  • the concentration of the formoterol salt ranges from 0.001 to 0.05% w/w, preferably from 0.002 to 0.03% w/w, and more preferably from 0.0025 to 0.01 % w/w.
  • the pharmaceutically acceptable salt may be advantageously selected from fumarate, maleate, xinafoate and pamoate, preferably formoterol is in the form of fumarate, more preferably formoterol fumarate dihydrate.
  • beclometasone dipropionate may be used in the anhydrous form or as a solvate such as monohydrate form.
  • the concentration of BDP is comprised between 0.05 and 0.16% w/w, preferably between 0.06 and 0.12% w/w, and more preferably between 0.07 and 0.10% w/w.
  • This finding contributes to increase the physical stability of the suspended particles of the formoterol salt over a prolonged period time.
  • the particle size of a suspended drug is controlled by the size to which the solid medicament is reduced by micronisation, while that of the dissolved drug is controlled by the size of the droplets generated upon actuation of the inhaler.
  • the formulation of the invention upon actuation of the inhaler, is highly efficacious, in particular for the treatment of mild persistent asthma, yielding particles of formoterol with a MMAD in the range 2-5 ⁇ m which are known to be more potent bronchodilators, and particles of BDP with a smaller MMAD ( ⁇ 1.5 ⁇ m) that may easily reach the bronchioloalveolar distal part of the respiratory tree wherein inflammation is known to play a role in spontaneous exacerbations of asthma symptoms.
  • the aerosol formulation of the invention could utilize HFA134a as the sole propellant which exhibits a higher vapor pressure.
  • a higher pressure may lead to more efficient atomization and finer sprays.
  • the advantages of the invention in some or all of its embodiments include the fact that the aerosol formulation of the invention is environmentally friendly, chemically more stable than the formulation of the prior art, less susceptible to Ostwald ripening, and hence physically stable, could deliver a high respirable fraction, due to the low content of ethanol, and could be easily and/or economically manufactured.
  • the vehicle of the formulation comprises a mixture of HFA134a and ethanol.
  • the polarity of said vehicle is comprised between about 9.5 and about 11.0, more preferably between about 9.5 and about 10.5 expressed as dielectric constant.
  • the amount of ethanol should be comprised between 2.0 and 4.8% w/w. Preferably said amount is comprised between 2.2 and 4.5% w/w, more preferably between 2.5% and 4.0% w/w, even more preferably between 2.6% and 3.5% w/w.
  • said amount may be comprised between 3.0 and 3.5% w/w.
  • the formulation of the invention may be suitable for delivering a therapeutic amount of the formoterol salt and beclometasone dipropionate in one or two actuations (shots) of the inhaler.
  • the formulations will be suitable for delivering 6-12 ⁇ g formoterol (as fumarate dihydrate) per actuation, especially 6 ⁇ g or 12 ⁇ g per actuation, and 50-200 ⁇ g beclometasone dipropionate per actuation, especially 50 or 100 ⁇ g per actuation.
  • the formulation according to the invention will be used in association with a suitable metering valve.
  • the formulation may be actuated by a metering valve capable of delivering a volume of between 50 ⁇ l and 100 ⁇ l, e.g. 50 ⁇ l or 63 ⁇ l or 100 ⁇ l.
  • the low amount of ethanol acts as a co-solvent for dissolving BDP but also assists the physical stability of the formulation.
  • the formulation of the invention may also comprise further active ingredients suitable for inhalation such as muscarinic receptor antagonists and PDE4 inhibitors.
  • the pharmaceutical formulation according to the invention may be filled into canisters suitable for delivering pharmaceutical aerosol formulations.
  • Canisters generally comprise a container such as plastic or plastic-coated glass bottle or preferably a metal can, for example an aluminum can which may optionally be anodized, lacquer-coated and/or plastic-coated, which container is closed with a metering valve.
  • aluminum cans are utilized such those commercially available, for instance, from Presspart.
  • the metering valves incorporate a gasket to prevent leakage of propellant through the valve.
  • the gasket may comprise any suitable elastomeric material such as for example low density polyethylene, chlorobutyl, black and white butadiene-acrylonitrile rubbers, butyl rubber, neoprene, EPDM (e.g. as described in WO95/02651 ) and TPE (thermoplastic elastomer; e.g. described in WO 92/11190 ). EPDM rubbers are preferred.
  • Suitable valves are commercially available from known manufacturers, for example, from Valois, France, Bespak plc UK, 3M, Neotechnic Ltd UK. Preferably the Bespack valves sold under the code 000100200376 are utilized.
  • Suitable channeling devices comprise, for example a valve actuator and a cylindrical or cone-like passage through which medicament may be delivered from the filled canister via the metering valve to the mouth of a patient e.g. a mouthpiece actuator.
  • valve stem is seated in a nozzle block which has an orifice leading to an expansion chamber.
  • the expansion chamber has an exit orifice which extends into the mouthpiece.
  • Actuator (exit) orifice having a diameter in the range 0.15-0.45 mm and a length from 0.30 to 1.7 mm are generally suitable.
  • an orifice having a diameter from 0.2 to 0.44 mm may be used, e.g. 0.22, 0.25, 0.30, 0.33 or 0.42 mm.
  • a material within the packaging which is able to adsorb any propellant and co-solvent which may leak from the canister (e.g. a molecular sieve).
  • the pMDI device filled with the formulation of the invention may be utilized together with suitable auxiliary devices favoring the correct use of the inhaler.
  • auxiliary devices are commercially available and, depending on their shape and size, are known as "spacers", “reservoirs” or “expansion chambers”.
  • VolumaticTM is, for instance, one of the most known and used reservoir, while AerochamberTM is one of the most used and known spacer.
  • a suitable expansion chamber is reported for example in WO 01/49350 .
  • the pMDI device may also be equipped with a dose counter or a dose indicator, which counts the number of administered doses and displays either numerically or by some other means the number of remaining doses, so that the patient will be aware when the drug canister has delivered its prescribed contents.
  • a dose counter or a dose indicator which counts the number of administered doses and displays either numerically or by some other means the number of remaining doses, so that the patient will be aware when the drug canister has delivered its prescribed contents.
  • the formulation of the invention may also be used with common pressurized breath-activated inhalers such as those known with the registered names of Easi-BreatheTM and AutohalerTM.
  • Administration of the aerosol formulation of the invention may be indicated for the prevention and/or treatment of mild, moderate or severe acute or chronic symptoms or for prophylactic treatment of respiratory diseases such as asthma and chronic obstructive pulmonary disease (COPD).
  • respiratory diseases such as asthma and chronic obstructive pulmonary disease (COPD).
  • COPD chronic obstructive pulmonary disease
  • Other respiratory disorders characterized by obstruction of the peripheral airways as a result of inflammation and presence of mucus such as chronic obstructive bronchiolitis and chronic bronchitis may also benefit by this kind of formulation.
  • the aerosol formulation of the invention may be indicated for controlling symptoms in patients affected by mild persistent asthma.
  • solubility of BDP in the HFA134a/ethanol mixtures was determined according the method reported in Gupta A et al J Aerosol Medicine 2003, 16(2), 167-174 , slightly modified as follows.
  • Vials that contained excess BDP were prepared at 2%, 3%, 4% and 5% ethanol in HFA134a.
  • the samples were filtered though a 0.2 ⁇ m PTFE filter coupled inline with Presspart standard C126 canisters fitted Bespak EPDM with a dip tube.
  • the formoterol fumarate dihydrate solubility at 20°C without BDP turned out to be about 0.005 ⁇ g/ ⁇ l corresponding to about 0.0005% w/w.
  • the formoterol fumarate dihydrate solubility at 20°C without BDP turned out to be about 0.03 ⁇ g/ ⁇ l corresponding to 0.003% w/w, and it does not change in the presence of BDP.
  • the formoterol fumarate dihydrate solubility at 20°C without BDP turned out to be about 0.006 ⁇ g/ ⁇ l corresponding to 0.0006% w/w, and it does not change in the presence of BDP.
  • An aerosol formulation was prepared starting from micronized formoterol fumarate dihydrate obtained by milling having a MMD comprised between 2 and micron and beclometasone dipropionate as commercially available.
  • Said formulation has the following composition: Formoterol fumarate dihydrate 0.0095% w/w Beclometasone dipropionate 0.079% w/w Ethanol 2.7% w/w HFA134 to 100%
  • This formulation was filled into an aluminum canister under pressure and fitted with a metering valve having a 63 ⁇ l metering chamber.
  • the solutions of the invention are capable of providing, upon actuation of the pMDI device in which they are contained, a FPF much higher than 50% for both the active ingredients.
  • An aerosol formulation is prepared with the following composition: Formoterol fumarate dihydrate 0.006% w/w Beclometasone dipropionate 0.1% w/w Ethanol 3.0% w/w HFA134 to 100%l
  • This formulation is filled into an aluminum canister under pressure and fitted with a metering valve having a 100 ⁇ l metering chamber.
  • An aerosol formulation may be prepared with the following composition: Formoterol fumarate dihydrate 0.012% w/w Beclometasone dipropionate 0.1% w/w Ethanol 3.0% w/w HFA134 to 100%
  • This formulation is filled into an aluminum canister under pressure and fitted with a metering valve having a 50 ⁇ l metering chamber.
  • An aerosol formulation is prepared with the following composition: Formoterol fumarate dihydrate 0.019% w/w Beclometasone dipropionate 0.16% w/w Ethanol 4.7% w/w HFA134 to 100%
  • This formulation is filled into an aluminum canister under pressure and fitted with a metering valve having a 63 ⁇ l metering chamber.
  • An aerosol formulation is prepared with the following composition: Formoterol fumarate dihydrate 0.0095% w/w Beclometasone dipropionate 0.079% w/w Ethanol 2.0% w/w HFA134 to 100%
  • This formulation is filled into an aluminum canister under pressure and fitted with a metering valve having a 63 ⁇ l metering chamber.

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EP14153337.2A 2009-10-02 2010-09-27 Pharmaceutical aerosol formulations of formoterol and beclometasone dipropionate Active EP2727582B1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
SI201031156A SI2727582T1 (sl) 2009-10-02 2010-09-27 Farmacevtske aerosolne formulacije formoterola in beklometazon dipropionata
EP14153337.2A EP2727582B1 (en) 2009-10-02 2010-09-27 Pharmaceutical aerosol formulations of formoterol and beclometasone dipropionate
MEP-2016-85A ME02398B (me) 2009-10-02 2010-09-27 Farmaceutske aerosolne formulacije formoterola i beklometazon dipropionata
PL14153337T PL2727582T3 (pl) 2009-10-02 2010-09-27 Farmaceutyczne formulacje aerozolowe formoterolu i dipropionianu beklometazonu
HRP20160630TT HRP20160630T1 (hr) 2009-10-02 2016-06-08 Farmaceutske aerosolne formulacije formoterola i beklometazon-dipropionata

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP09172083 2009-10-02
EP14153337.2A EP2727582B1 (en) 2009-10-02 2010-09-27 Pharmaceutical aerosol formulations of formoterol and beclometasone dipropionate
EP10763317.4A EP2482799B1 (en) 2009-10-02 2010-09-27 Pharmaceutical aerosol formulations of formoterol and beclometasone dipropionate

Related Parent Applications (2)

Application Number Title Priority Date Filing Date
EP10763317.4A Division EP2482799B1 (en) 2009-10-02 2010-09-27 Pharmaceutical aerosol formulations of formoterol and beclometasone dipropionate
EP10763317.4A Division-Into EP2482799B1 (en) 2009-10-02 2010-09-27 Pharmaceutical aerosol formulations of formoterol and beclometasone dipropionate

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EP2727582A1 EP2727582A1 (en) 2014-05-07
EP2727582B1 true EP2727582B1 (en) 2016-03-16

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EP14153337.2A Active EP2727582B1 (en) 2009-10-02 2010-09-27 Pharmaceutical aerosol formulations of formoterol and beclometasone dipropionate
EP10763317.4A Active EP2482799B1 (en) 2009-10-02 2010-09-27 Pharmaceutical aerosol formulations of formoterol and beclometasone dipropionate

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EP (2) EP2727582B1 (pl)
KR (1) KR101778814B1 (pl)
CN (2) CN103919785B (pl)
AR (2) AR078494A1 (pl)
BR (1) BR112012007484A2 (pl)
CA (1) CA2776266C (pl)
CY (2) CY1115266T1 (pl)
DK (2) DK2482799T3 (pl)
ES (2) ES2487626T3 (pl)
HK (2) HK1199214A1 (pl)
HR (2) HRP20140818T1 (pl)
HU (1) HUE029159T2 (pl)
JO (1) JO3024B1 (pl)
ME (1) ME02398B (pl)
PL (2) PL2727582T3 (pl)
PT (1) PT2482799E (pl)
RS (2) RS53514B1 (pl)
RU (1) RU2650175C2 (pl)
SI (2) SI2727582T1 (pl)
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WO (1) WO2011038872A1 (pl)

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US9119777B2 (en) * 2008-05-30 2015-09-01 Microdose Therapeutx, Inc. Methods and compositions for administration of oxybutynin
ES2683254T3 (es) * 2012-01-25 2018-09-25 Chiesi Farmaceutici S.P.A. Formulación en polvo seca que comprende un corticoesteroide y un beta-adrenérgico para administración por inhalación
US11052202B2 (en) * 2012-11-07 2021-07-06 Chiesi Farmaceutici S.P.A. Drug delivery device for the treatment of patients with respiratory diseases
BR112018011266B1 (pt) 2015-12-04 2023-11-21 Mexichem Fluor S.A. De C.V. Composição farmacêutica, recipiente vedado, e, métodos para tratar um paciente que sofre ou é propenso a sofrer de um distúrbio respiratório e para estabilizar uma composição farmacêutica
CN112438966B (zh) * 2019-08-30 2022-08-26 四川普锐特药业有限公司 一种医用定量吸入气雾剂

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US5290539A (en) 1990-12-21 1994-03-01 Minnesota Mining And Manufacturing Company Device for delivering an aerosol
CA2166970C (en) 1993-07-15 2000-12-19 Oh-Seung Kwon Seals for use in an aerosol delivery device
GB9612297D0 (en) * 1996-06-11 1996-08-14 Minnesota Mining & Mfg Medicinal aerosol formulations
US6423298B2 (en) * 1998-06-18 2002-07-23 Boehringer Ingelheim Pharmaceuticals, Inc. Pharmaceutical formulations for aerosols with two or more active substances
SE9900833D0 (sv) * 1999-03-09 1999-03-09 Astra Ab Novel combination
IT1317720B1 (it) 2000-01-07 2003-07-15 Chiesi Farma Spa Dispositivo per la somministrazione di aerosol dosati pressurizzati inpropellenti idrofluoroalcani.
CZ303833B6 (cs) 2000-05-22 2013-05-22 Chiesi Farmaceutici S.P.A. Aerosolový prostredek
US6472563B1 (en) * 2001-11-09 2002-10-29 Sepracor Inc. Formoterol tartrate process and polymorph
GB0205327D0 (en) * 2002-03-06 2002-04-17 Glaxo Group Ltd compounds
GB0323685D0 (en) * 2003-10-09 2003-11-12 Jagotec Ag Improvements in or relating to organic compounds
EP1982709A1 (en) * 2007-04-19 2008-10-22 CHIESI FARMACEUTICI S.p.A. Use of a composition comprising formoterol and beclomethasone dipropionate for the prevention or treatment of an acute condition of asthma
RU2356537C2 (ru) * 2007-07-25 2009-05-27 Закрытое Акционерное Общество (ЗАО) "Пульмомед" Фармацевтический состав дозированных аэрозолей, содержащий противоастматические лекарственные средства в виде суспензий, растворов, эмульсий, растворов и эмульсий

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RU2012112454A (ru) 2013-11-10
AR078494A1 (es) 2011-11-09
CA2776266C (en) 2017-11-28
KR101778814B1 (ko) 2017-09-15
HRP20140818T1 (hr) 2014-10-10
CY1117596T1 (el) 2017-04-26
CN102548537B (zh) 2014-06-25
JO3024B1 (ar) 2016-09-05
CN102548537A (zh) 2012-07-04
PL2482799T3 (pl) 2014-11-28
CN103919785A (zh) 2014-07-16
BR112012007484A2 (pt) 2020-06-09
HK1199214A1 (en) 2015-06-26
RS53514B1 (en) 2015-02-27
SI2482799T1 (sl) 2014-10-30
ME02398B (me) 2016-09-20
HRP20160630T1 (hr) 2016-07-01
US8420060B2 (en) 2013-04-16
CN103919785B (zh) 2016-08-24
US20110081301A1 (en) 2011-04-07
RU2650175C2 (ru) 2018-04-10
HUE029159T2 (hu) 2017-02-28
KR20120100901A (ko) 2012-09-12
CY1115266T1 (el) 2017-01-04
ES2487626T3 (es) 2014-08-22
EP2482799B1 (en) 2014-06-18
TW201119644A (en) 2011-06-16
AR123674A2 (es) 2023-01-04
SI2727582T1 (sl) 2016-05-31
EP2482799A1 (en) 2012-08-08
TWI449523B (zh) 2014-08-21
WO2011038872A1 (en) 2011-04-07
ES2568913T3 (es) 2016-05-05
RS54721B1 (en) 2016-08-31
DK2727582T3 (en) 2016-05-17
HK1167817A1 (en) 2012-12-14
EP2727582A1 (en) 2014-05-07
PT2482799E (pt) 2014-08-06
CA2776266A1 (en) 2011-04-07
PL2727582T3 (pl) 2016-06-30
DK2482799T3 (da) 2014-09-01

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